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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762963Generated: October 30, 2026

Acetic Anhydride → 1-Acetyl-7-(benzyloxy)-1H-indole-4-carbaldehyde

https://huagongshe.com/reaction/1762963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant7-(Benzyloxy)-1H-indole-4-carbaldehydeHCID 13243486—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-7-(benzyloxy)-1H-indole-4-carbaldehydeHCID 13243487—

Reaction Steps

500 mg of 7-benzyloxy-4-formylindole is combined with 50 mg of 4-dimethylaminopyridine, 0.7 ml of triethylamine, 0.5 ml of acetic anhydride, and 10 ml of dichloromethane and agitated for 24 hours at room temperature. The reaction mixture is then diluted with 50 ml of dichloromethane, washed with concentrated sodium bicarbonate solution; the organic phase is dried and concentrated. The residue is recrystallized from isopropanol, thus obtaining 400 mg of 1-acetyl-7-benzyloxy-4-formylindole, mp 77°-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835175
Source datasetuspto-grants-1989_05
ORD IDord-1271ca2d44dc4500b5e5364331e39618
Source noteuspto-grants-1989_05